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利用抑制差减杂交技术鉴定桃芽休眠解除相关基因。

Identification of genes associated with bud dormancy release in Prunus persica by suppression subtractive hybridization.

机构信息

Instituto Valenciano de Investigaciones Agrarias, E-46113, Moncada, Valencia, Spain.

出版信息

Tree Physiol. 2010 May;30(5):655-66. doi: 10.1093/treephys/tpq008. Epub 2010 Mar 15.

Abstract

To better understand the molecular and physiological mechanisms underlying maintenance and release of seasonal bud dormancy in perennial trees, we identified differentially expressed genes during dormancy progression in reproductive buds from peach (Prunus persica [L.] Batsch) by suppression subtractive hybridization (SSH) and microarray hybridization. Four SSH libraries were constructed, which were respectively enriched in cDNA highly expressed in dormant buds (named DR), in dormancy-released buds (RD) and in the cultivars with different chilling requirement, 'Zincal 5' (ZS) and 'Springlady' (SZ), sampled after dormancy release. About 2500 clones picked from the four libraries were loaded on a glass microarray. Hybridization of microarrays with the final products of SSH procedure was performed in order to validate the selected clones that were effectively enriched in their respective sample. Nearly 400 positive clones were sequenced, which corresponded to 101 different unigenes with diverse functional annotation. We obtained DAM4, 5 and 6 genes coding for MADS-box transcription factors previously related to growth cessation and terminal bud formation in the evergrowing mutant of peach. Several other cDNAs are similar to dormancy factors described in other species, and others have been related to bud dormancy for the first time in this study. Quantitative reverse transcription polymerase chain reaction analysis confirmed differential expression of cDNAs coding for a Zn-finger transcription factor, a GRAS-like regulator, a DNA-binding protein and proteins similar to forisome subunits involved in the reversible occlusion of sieve elements in Fabaceae, among others.

摘要

为了更好地理解多年生树木季节性芽休眠维持和释放的分子和生理机制,我们通过抑制消减杂交(SSH)和微阵列杂交鉴定了桃(Prunus persica [L.] Batsch)生殖芽休眠进程中差异表达的基因。构建了 4 个 SSH 文库,分别富集了在休眠芽中高度表达的 cDNA(命名为 DR)、在休眠释放芽中表达的 cDNA(RD)和在不同需冷量品种 'Zincal 5'(ZS)和 'Springlady'(SZ)中表达的 cDNA。从这 4 个文库中随机挑取了约 2500 个克隆并点样到玻璃微阵列上。为了验证在各自样本中有效富集的选定克隆,用 SSH 程序的最终产物进行了微阵列杂交。对近 400 个阳性克隆进行测序,得到了 101 个不同功能注释的不同的单基因。我们获得了编码 MADS 框转录因子的 DAM4、5 和 6 个基因,这些基因先前与桃的不断生长突变体中的生长停止和顶芽形成有关。其他一些 cDNA 与其他物种中描述的休眠因子相似,还有一些在这项研究中首次与芽休眠有关。定量反转录聚合酶链反应分析证实了编码锌指转录因子、GRAS 样调节剂、DNA 结合蛋白和类似于豆科可逆闭塞筛管的类蛋白的 cDNA 的差异表达。

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